Package 63187-602-30

Brand: losartan potassium and hydrochlorothiazide

Generic: losartan potassium and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 63187-602-30
Digits Only 6318760230
Product NDC 63187-602
Description

30 TABLET, FILM COATED in 1 BOTTLE (63187-602-30)

Marketing

Marketing Status
Marketed Since 2018-12-01
Brand losartan potassium and hydrochlorothiazide
Generic losartan potassium and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c925be88-1cf9-4631-9d10-d6cca5e94765", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468", "979471"], "spl_set_id": ["198d5151-7982-4639-9fe1-6573a4529348"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-602-30)", "package_ndc": "63187-602-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-602-60)", "package_ndc": "63187-602-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-602-90)", "package_ndc": "63187-602-90", "marketing_start_date": "20181201"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "63187-602_c925be88-1cf9-4631-9d10-d6cca5e94765", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "63187-602", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}